In wild-type leaves (Figure 7C). In the presence of lincomycin, the

In wild-type leaves (Lecirelin Figure 7C). In the presence of lincomycin, the decline in Fv/Fm in the cplepa mutants was similar to that observed in the wild-type leaves during the same photoinhibitory light treatment (Figure 7C). Because lincomycin blocks the repair of PSII by inhibiting de novo chloroplast protein synthesis, these resultsFigure 3. Identification and Phenotyping of the cplepa Mutants. A: T-DNA insertion sites in the cpLEPA gene. Exons are indicated by black boxes, introns by lines, and the T-DNA insertions by vertical arrows. The horizontal arrows illustrate the primers used for T-DNA insertion verification and RT-PCR. The scale bar indicates 500 bp. B: RT-PCR analysis. RT-PCR was performed using specific primers for cpLEPA 18334597 or ACTIN. C: Two-week-old WT and cplepa-1 mutants grown on MS medium supplied with 0, 1 sucrose and 2 sucrose. D: Complementation of the cplepa-1 mutant. The cDNA of the cpLEPA gene was cloned into a binary plant transformation vector and used for complementation of the cplepa-1 11089-65-9 mutant (cplepa-1/ 35S::cpLEPA). Four-week-old WT, cplepa-1, cplepa-2 and cplepa-1/35S::cpLEPA plants were grown on soil. Fluorescence was measured with a CF Imager and visualized using a pseudocolor index, as indicated at the bottom, Fm and Fv/Fm value were presented. E: Growth of wild-type and cplepa-1 mutant plants on soil at 120 mmol m22 s21. The values shown are averages 6 s.e. (n = 6). doi:10.1371/journal.pone.0049746.gcpLEPA in Chloroplast TranslationTable 1. Chlorophyll Contents in Wild-Type and cplepa-1 Plants.chlorophyll Chl a Chl b Chl a+b Chl a/Chl bWT 792.6617 261.4612 1083.8631 360.cplepa-699.6612 261.1611 963.7614 2.660.cplepa-1/WT( )88 100 89doi:10.1371/journal.pone.0049746.tsuggest that the mutant’s sensitivity to high light is due to an impaired PSII repair process.DiscussionLEPA is an extremely conserved and widely distributed translation factor [11]. The amino acid sequence of Arabidopsis cpLEPA shows 64 amino acid identity 1676428 with that of E. coli LEPA (Figure 1). This degree of sequence conservation is particularly high for a comparison between higher plants and bacteria. CpLEPA contains four domains: LEPA, LEPA-II, LEPA-C and a CTD domain. The LEPA and LEPA-II domains contain the extremely conserved key amino acids that are important for GTP binding, which are known as the G1, G2, G3 and G4 sequence motifs. The G1, G3 and G4 motifs are responsible for binding and hydrolyzing GTP and for interacting with the cofactor Mg2+ [12]. The G2 motif undergoes a conformational change that is essential for GTPase function [13]. LEPA-C was predicted to function in translation elongation. The structure and sequence similarity of cpLEPA to E. coli LEPA indicates a role for this protein in the efficiency of chloroplast protein translation. LEPA was initially reported as the leader peptide of the lep operon and was described as a membrane-associated GTPbinding protein [4]. The N-terminal 51 amino acids of Arabidopsis cpLEPA was hypothesized to function as a chloroplast signal peptide (Figure 1). Immunoblot analysis verified that cpLEPA is located in the chloroplast and is primarily found in association with the thylakoid membrane. Membrane-associated cpLEPA could be washed out by Na2CO3 and CaCl2, indicating that cpLEPA is not an integral membrane protein and that the association with the membrane is flexible (Figure 2). Pech et al suggested that the membrane acts as a storage depot for LEPA and that LEPA is released into the cyto.In wild-type leaves (Figure 7C). In the presence of lincomycin, the decline in Fv/Fm in the cplepa mutants was similar to that observed in the wild-type leaves during the same photoinhibitory light treatment (Figure 7C). Because lincomycin blocks the repair of PSII by inhibiting de novo chloroplast protein synthesis, these resultsFigure 3. Identification and Phenotyping of the cplepa Mutants. A: T-DNA insertion sites in the cpLEPA gene. Exons are indicated by black boxes, introns by lines, and the T-DNA insertions by vertical arrows. The horizontal arrows illustrate the primers used for T-DNA insertion verification and RT-PCR. The scale bar indicates 500 bp. B: RT-PCR analysis. RT-PCR was performed using specific primers for cpLEPA 18334597 or ACTIN. C: Two-week-old WT and cplepa-1 mutants grown on MS medium supplied with 0, 1 sucrose and 2 sucrose. D: Complementation of the cplepa-1 mutant. The cDNA of the cpLEPA gene was cloned into a binary plant transformation vector and used for complementation of the cplepa-1 mutant (cplepa-1/ 35S::cpLEPA). Four-week-old WT, cplepa-1, cplepa-2 and cplepa-1/35S::cpLEPA plants were grown on soil. Fluorescence was measured with a CF Imager and visualized using a pseudocolor index, as indicated at the bottom, Fm and Fv/Fm value were presented. E: Growth of wild-type and cplepa-1 mutant plants on soil at 120 mmol m22 s21. The values shown are averages 6 s.e. (n = 6). doi:10.1371/journal.pone.0049746.gcpLEPA in Chloroplast TranslationTable 1. Chlorophyll Contents in Wild-Type and cplepa-1 Plants.chlorophyll Chl a Chl b Chl a+b Chl a/Chl bWT 792.6617 261.4612 1083.8631 360.cplepa-699.6612 261.1611 963.7614 2.660.cplepa-1/WT( )88 100 89doi:10.1371/journal.pone.0049746.tsuggest that the mutant’s sensitivity to high light is due to an impaired PSII repair process.DiscussionLEPA is an extremely conserved and widely distributed translation factor [11]. The amino acid sequence of Arabidopsis cpLEPA shows 64 amino acid identity 1676428 with that of E. coli LEPA (Figure 1). This degree of sequence conservation is particularly high for a comparison between higher plants and bacteria. CpLEPA contains four domains: LEPA, LEPA-II, LEPA-C and a CTD domain. The LEPA and LEPA-II domains contain the extremely conserved key amino acids that are important for GTP binding, which are known as the G1, G2, G3 and G4 sequence motifs. The G1, G3 and G4 motifs are responsible for binding and hydrolyzing GTP and for interacting with the cofactor Mg2+ [12]. The G2 motif undergoes a conformational change that is essential for GTPase function [13]. LEPA-C was predicted to function in translation elongation. The structure and sequence similarity of cpLEPA to E. coli LEPA indicates a role for this protein in the efficiency of chloroplast protein translation. LEPA was initially reported as the leader peptide of the lep operon and was described as a membrane-associated GTPbinding protein [4]. The N-terminal 51 amino acids of Arabidopsis cpLEPA was hypothesized to function as a chloroplast signal peptide (Figure 1). Immunoblot analysis verified that cpLEPA is located in the chloroplast and is primarily found in association with the thylakoid membrane. Membrane-associated cpLEPA could be washed out by Na2CO3 and CaCl2, indicating that cpLEPA is not an integral membrane protein and that the association with the membrane is flexible (Figure 2). Pech et al suggested that the membrane acts as a storage depot for LEPA and that LEPA is released into the cyto.